FDAApril 9, 2021device

ADULT CHEST TUBE TRAY. Medical convenience kit, Avid Medical Part Number: LAKC001-04

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator. Under certain circumstances the applicator may grow Aspergillus penicillioides, which may result in a breach of the package integrity. A breach of package integrity may contaminate other components in AVID Medical kits.

What to do

FDA enforcement status: Terminated

Brands named

avid medicalavid

UPCs

208091602610162080916029313020809160313005

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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